A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544568



Internal ID20917807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63423036..63884116hg38UCSC Ensembl
chr2:63650171..64111250hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38461081
hg19461080
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258755
Samples
Known GenesMDH1, UGP2, WDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544568
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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